Mongolian spot

Slate grey nevus

Other names: Mongolian spot, Mongolian blue spot, congenital dermal melanocytosis,[1] dermal melanocytosis[1]
Infant with slate grey nevus
Specialty| Dermatology

A mongolian spot, also known as slate grey nevus or congenital dermal melanocytosis, is a benign, flat, congenital birthmark with wavy borders and an irregular shape. In 1883, it was described and named after Mongolians by Erwin Bälz, a German anthropologist based in Japan, who erroneously believed it to be most prevalent among his Mongolian patients.[2][3][4][5] It normally disappears three to five years after birth and almost always by puberty. The most common color is blue, although they can be blue-gray, blue-black or deep brown.

It is common and occurs in around 10% of white babies, 40% to 70% of Hispanic babies, 81% of Asian babies, and 98% of African American babies.[6]

## Contents

* 1 Symptoms and signs
* 2 Cause
* 2.1 Anthropological description
* 3 Treatment
* 4 Prevalence
* 5 Cultural terminology
* 6 See also
* 7 References
* 8 External links

## Symptoms and signs[edit | edit source]

Mongolian spot

The Mongolian spot is usually flat, and has a color that varies between blue-grey or brown on the individual. Furthermore can appear as a single or multiple spots on said individual [7]

## Cause[edit | edit source]

Mongolian spot is a congenital developmental condition—that is, one existing from birth—exclusively involving the skin. The blue colour is caused by melanocytes, melanin-containing cells, that are usually located in the surface of the skin (the epidermis), but are in the deeper region (the dermis) in the location of the spot.[8] Usually, as multiple spots or one large patch, it covers one or more of the lumbosacral area (lower back), the buttocks, sides, and shoulders.[8] It results from the entrapment of melanocytes in the lower half to two-thirds of the dermis during their migration from the neural crest to the epidermis during embryonic development.[8]

Male and female infants are equally predisposed to slate grey nevus.[9][10][11] People who are not aware of the background of the slate grey nevus may mistake them for bruises, possibly resulting in mistaken concerns about abuse.[12][13][14]

### Anthropological description[edit | edit source]

The French anthropologist Robert Gessain interested himself in what he called the tache pigmentaire congenitale or coloured birthmark, publishing multiple papers in the Journal de la Société des Américanistes, an academic journal covering the cultural anthropology of the Americas. Gessain spent time with the Huehuetla Tepehua people in Hidalgo, Mexico, and wrote in 1947 about the spot's "location, shape, colour, histology, chemistry, genetic transmission, and racial distribution". He had previously spent several winters in Greenland, and wrote an overview in 1953 of what was known about the spot. He hypothesised that the age at which it faded in various populations might prove to be a distinguishing characteristic of those groups. Gessain claimed that the spot was first observed amongst the Inuit.[15]

Hans Egede Saabye, a Danish priest and botanist, spent 1770–1778 in Greenland. His diaries, published in 1816 and translated into several European languages, contained much ethnographic information. He described the spot on newborns, saying he had seen it often when the infants were presented naked for baptism. A second Danish observer was doctor and zoologist Daniel Frederik Eschricht, mainly based in Copenhagen. In 1849 he wrote of the "mixed" babies he had delivered at the lying-in hospital. He also says that "the observation made for the first time by Saabye about Inuit children has been completely confirmed by Captain Holbøll", who sent him a fetus pickled in alcohol.[15]

Gessain goes on to state that it was only in 1883 that an anthropologist mentions the spot. It was Erwin Bälz, a German working in Tokyo, who described a dark blue mark on Japanese infants. He presented his findings in 1901 in Berlin, and from that point on, Bälz's name was associated with certain skin cells containing pigment. Captain Gustav Frederik Holm wrote in 1887 that his Greenlandic interpreter Johannes Hansen (known as Hanserak) attested to the existence of the birthmark over the kidney region of newborns, which grows larger as they grow older. That year, the Danish anthropologist Soren Hansen drew the connection between the observations of Bälz in Japan and Saabye in Greenland. "This cannot be a coincidence. It is not the first time that the resemblance between the Japanese and the Eskimo has been pointed out." Fridtjof Nansen, the Norwegian polar explorer, said that the spot was widespread in the mixed Danish-Inuit population of West Greenland. Soren Hansen confirmed this. A missionary in Bethel, Alaska, a traditional gathering place of Yup'ik people, reported that the spots were common on children. Rudolf Trebitsch, an Austrian linguist and ethnologist, spent the summer of 1906 on the West Coast of Greenland, and listed all the examples he came across. Gessain went to north Labrador in 1926, looking for children with these spots. In 1953 Dr Saxtorph, medical advisor to the Greenland department (part of the Danish government), wrote that the Greenlanders do not like outsiders to see or discuss these birthmarks; "they doubtless feel as a reminiscence of the time when they lived on a low cultural level".[15]

The presence or absence of the slate grey nevus was used by racial theorists such as Joseph Deniker (1852-1918), the French anthropologist.[16]

The Journal of Cutaneous Diseases Including Syphilis, Volume 23 contained several accounts of the slate grey nevus on children in the Americas:

> Holm ("Ethnological Sketch. Communications on Greenland," X., Copenhagen, 1887) announced the presence of the spot in the east part of Greenland. Bartels ("The So-Called 'Mongolian' Spots on Infants of Esquimaux," Ethnologic Review, 1903) received letters regarding it from East Greenland and also from Esquimaux of Alaska. In half-breed European-Esquimaux, Hansen says he has encountered it. Among Indians of North Vancouver, British Columbia, there are observations made by Baelz as well as by Tenkate (secondhand). In the Mayas of Central America, Starr's (Data on the Ethnography of Western Mexico, Part H., 1902) facts are corroborated by Herman (Aparecimiento de la Mancha Mongolica. Revista de Ethnologia, 1904). He cites A. F. Chamberlain (Pigmentary Spots, American Anthropologist, 1902,) and Starr (Sacral Spots of Mayan Indians, Science, New Series, xvii., 1903).

In Central America, according to these authorities, the spot is called Uits, "pan," and it is an insult to speak of it. It disappears in the tenth month. It is bluish-reddish (in these Native people), and is remarkable by its small size. The mulberry colored spot is very well known in Afro-Brazilians. In Brazil, among individuals of mixed Indigenous American and West African descent (pardo) it is called "genipapo", from its resemblance in color (bluish-gray) to an indigenous fruit of Brazil, named genipapo (a Native word adopted into Portuguese).

## Treatment[edit | edit source]

As a congenital benign nevus, Mongolian spots do not require treatment and in most cases disappear before adolescence. No cases of malignant degeneration have been reported.

## Prevalence[edit | edit source]

Infants may be born with one or more slate grey nevus ranging from small area on the buttocks to a larger area on the back. The birthmark is prevalent among East, South, Southeast, North and Central Asian peoples, Indigenous Oceanians (chiefly Micronesians and Polynesians), certain populations in Africa,[17] Amerindians,[18] non-European Latin Americans and Caribbeans of mixed-race descent.[8][19][20]

They occur in around 80%[21] of Asians, and 80%[21] to 85% of Native American infants.[19] Approximately 90% of Polynesians and Micronesians are born with slate grey nevus, as are about 46% of children in Latin America,[22] where they are associated with non-European descent. These spots also appear on 5–10% of babies of full Caucasian descent; Coria del Río in Spain has a high incidence due to the presence of descendants of members of the delegation led by Hasekura Tsunenaga, the first Japanese official envoy to Spain in the early 17th century.[19][23][better source needed] African American babies have slate grey nevus at a frequencies of 90%[21] to 96%.[24]

According to a 2006 study examining the Mongolian spot among newborns in the Turkish city of İzmir, it was found out that 26% of the examined babies had the condition. It was noted the prevalence rate was 20% and 31% in boys and girls, respectively. The study also reported that no children born with light hair had the mark, meanwhile 47% of the children with dark hair having it.[25]

Since the last century, extensive research has been made regarding the prevalence of said spot in populations of mixed European-Amerindian ancestry. A publication from 1905, citing field research made by the anthropologist Frederick Starr, states that the spot is not present in Mestizo populations,[26] however, if Starr's actual research is consulted it is observed the he declares that "seven Mayan children presented the spot, three mixed children didn't have it...",[27] Starr therefore does not make an absolute judgement, as he does not say how many mixed children were analyzed in total. Nowadays it is completely accepted that the big majority of Mexico's and Latin America's mixed-race populations have the Mongolian spot[28] and that its presence works as an indicator of the actual degree of mestizaje present in a given population,[29] having its lower frequency in Uruguay with 36%,[29] followed by Argentina with an incidence 44%,[30] Mexico with 50%-52%,[31] 68% on Hispanic-Americans[32] and 88% on highland Peruvians.[33]

A study performed in hospitals of Mexico City reported that, on average, 51.8% of Mexican newborns presented slate grey nevus, while it was absent on 48.2% of the analyzed babies.[30] According to the Mexican Social Security Institute nationwide, around half of Mexican babies have the slate grey nevus.[34]

Central American indigenous children were subjected to racism due to their slate grey nevus but progressive circles began to make having the slate grey nevus popular after the late 1960s.[35]

Highland Peruvians have the slate grey nevus.[36]

## Cultural terminology[edit | edit source]

The slate grey nevus is referred to in the Japanese idiom shiri ga aoi (尻が青い), meaning "to have a blue butt",[37][38] which is a reference to immaturity or inexperience.

* In Mongolian Language, it is known as "Хөх толбо".

* Korean mythology explains the nevus as a bruise formed when Samshin halmi or Samsin Halmoni (Korean: 삼신할머니), a shaman spirit to whom people pray around childbirth, slapped the baby's behind to hasten the baby to quickly get out from his or her mother's womb.

* In Chinese, it is referred to as "青痕" (Pinyin: Qīng Hén; Literally: Blue Mark). Among common folk it is said to be caused by the Buddhist goddess of childbirth Songzi Guanyin (Simplified Chinese: 送子观音; Pinyin: Sòng Zǐ Guān Yīn; Literally: The Goddess of Baby Sending) when she is slapping the babies backside telling it to be born. Others say it is because the baby does not want to leave the mother's womb so Songzi Guanyin will kick it out, leaving the bruise. While a small portion of people, wrongfully, believe it happens when the doctor is slapping the baby's backside to make it cry. Scientifically, it is also referred to as "蒙古斑" (Pinyin: Měng Gǔ Bān; Literally: Mongolian Spot)

* In Khmer, it is known as "khnau" (ខ្នៅ) which translates to 'Mongolian spot' as well as other skin conditions such as vitiligo and leucoderma.[39]
* The mark is also common among Maya people of the Yucatan Peninsula[40] where is referred to as Wa in Maya, which means "circle".

* In Ecuador, the native Indians of Colta are insultingly referred to in Spanish by a number of terms which allude to the slate grey nevus.[41]

* In Spanish it is called mancha mongólica and mancha de Baelz (see Erwin Bälz).[42]

## See also[edit | edit source]

* Nevus flammeus nuchae, also known as stork bite
* List of cutaneous conditions

## References[edit | edit source]

1. ↑ 1.0 1.1 Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 1720\. ISBN 978-1-4160-2999-1.
2. ↑ Die koerperlichen Eigenschaften der Japaner.(1885) Baelz.E. Mittheil.d.deusch Gesell.f.Natur-u-Voelkerheilkunde Ostasiens. Bd.4.H.32
3. ↑ Circumscribed dermal melanosis (Mongolian spot)(1981) Kikuchi I, Inoue S. in "Biology and Diseases of Dermal Pigmentation", University of Tokyo Press, p83
4. ↑ Bernard Cohen (1993). Atlas of pediatric dermatology. Wolfe. pp. 6–17. ISBN 978-1563750199. Archived from the original on August 28, 2021. Retrieved May 17, 2014.
5. ↑ JAMA: The Journal of the American Medical Association, Volume 51. American Medical Association. American Medical Association. 1908. p. 2262\. Archived from the original on August 28, 2021. Retrieved May 17, 2014.`{{cite book}}`: CS1 maint: others (link)
6. ↑ Onalaja, Amanda A.; Taylor, Susan C. (2021). "1. Defining skin color". In Li, Becky S.; Maibach, Howard I. (eds.). Ethnic Skin and Hair and Other Cultural Considerations. Switzerland: Springer. p. 9\. ISBN 978-3-030-64829-9. Archived from the original on 2022-09-15. Retrieved 2022-08-29.
7. ↑ "MONGOLIAN SPOT". aocd.org. Archived from the original on 23 September 2020. Retrieved 29 July 2021.
8. ↑ 8.0 8.1 8.2 8.3 Mongolian blue spots Archived January 19, 2017, at the Wayback Machine – Health care guide discussing the Mongolian blue spot.
9. ↑ Kroon, Susanne; Clemmensen, Ole Jacob; Hastrup, Nina (September 1987). "Incidence of congenital melanocytic nevi in newborn babies in Denmark". Journal of the American Academy of Dermatology. 17 (3): 422–426. doi:10.1016/s0190-9622(87)70223-0.
10. ↑ Paláu-Lázaro, M.C.; Buendía-Eisman, A.; Serrano-Ortega, S. (2008). "Prevalence of Congenital Nevus in 1000 Live Births in Granada, Spain". Actas Dermo-Sifiliográficas (English Edition). 99 (1): 81. doi:10.1016/s1578-2190(08)70202-6.
11. ↑ Alper, Joseph C.; Holmes, Lewis B. (July 1983). "The Incidence and Significance of Birthmarks in a Cohort of 4,641 Newborns". Pediatric Dermatology. 1 (1): 58–68. doi:10.1111/j.1525-1470.1983.tb01093.x.
12. ↑ Mongolian Spot Archived 2019-07-22 at the Wayback Machine \- English information of Mongolian spot, written by Hironao NUMABE, M.D., Tokyo Medical University.
13. ↑ Empson, Rebecca M. (2010). Harnessing fortune : personhood, memory and place in northeast Mongolia. Oxford: Oxford University Press. ISBN 9780197264737.
14. ↑ Robert M. Reece; Stephen Ludwig, eds. (2001). Child Abuse: Medical Diagnosis and Management (2, illustrated ed.). Lippincott Williams & Wilkins. p. 180\. ISBN 978-0781724449. Archived from the original on August 28, 2021. Retrieved May 17, 2014.
15. ↑ 15.0 15.1 15.2 Gessain, Robert (1953). "La tache pigmentaire congénitale chez les Eskimo d'Angmassalik" [Congenital pigment spot in the Eskimo people of Angmassalik] (PDF). Journal de la Société des Américanistes (in français). 42 (1): 301–332. doi:10.3406/jsa.1953.2408.`{{cite journal}}`: CS1 maint: url-status (link)
16. ↑ Deniker, J. (1901). "Les taches congénitales dans la région sacro-lombaire considérées comme caractère de race" [Congenital spots in the sacro-lumbar region considered to be a breed trait] (PDF). Bulletins de la Société d'anthropologie de Paris (in français). 2 (1): 274–281. doi:10.3406/bmsap.1901.5961.`{{cite journal}}`: CS1 maint: url-status (link)
17. ↑ Kevin C. Stuart (1997). Mongols in Western/American consciousness (illustrated ed.). Edwin Mellen Press. p. 95\. ISBN 978-0773484436. Archived from the original on August 28, 2021. Retrieved May 17, 2014.
18. ↑ Miller (1999). Nursing Care of Older Adults: Theory and Practice (3, illustrated ed.). Lippincott Williams & Wilkins. p. 90\. ISBN 978-0781720762. Archived from the original on April 14, 2021. Retrieved May 17, 2014.
19. ↑ 19.0 19.1 19.2 "About Mongolian Spot". tokyo-med.ac.jp. Archived from the original on December 8, 2008. Retrieved October 1, 2015.
20. ↑ "Transcultural Medicine: Dealing with patients from different cultures". Archived from the original on 2018-07-20. Retrieved 2021-07-12.
21. ↑ 21.0 21.1 21.2 Giger, Joyce Newman (2016). Transcultural Nursing – E-Book: Assessment and Intervention. Elsevier Health Sciences. p. 176\. ISBN 978-0323400046. Archived from the original on August 28, 2021. Retrieved September 14, 2017.
22. ↑ "Epidemiology of Mongolian spot on MedScape". Archived from the original on 2021-06-27. Retrieved 2021-07-12.
23. ↑ "Spain's Japon clan has reunion to trace its 17th century roots". The Japan Times. Archived from the original on January 15, 2013. Retrieved October 1, 2015.
24. ↑ N Silverberg (2012). Atlas of Pediatric Cutaneous Biodiversity: Comparative Dermatologic Atlas of Pediatric Skin of All Colors. Springer Science & Business Media. p. 34\. ISBN 978-1461435648. Archived from the original on August 28, 2021. Retrieved May 17, 2014.
25. ↑ Egemen A, Ikizoğlu T, Ergör S, Mete Asar G, Yilmaz O (July 2006). "Frequency and characteristics of Mongolian spots among Turkish children in Aegean region". Turk J Pediatr. 48 (3): 232–6. PMID 17172067.
26. ↑ Douglass W. Montgomery (1905). Journal of Cutaneous Diseases Including Syphilis Volume 23. Vol. 23\. American Dermatological Association. p. 210. Retrieved October 27, 2019.
27. ↑ Brennemann, Joseph (1907). "The Sacral or so-Called 'Mongolian' Pigment Spots of Earliest Infancy and Childhood, with Especial Reference to Their Occurrence in the American Negro". American Anthropologist. 9 (1): 12–30. doi:10.1525/aa.1907.9.1.02a00030.
28. ↑ Lawrence C. Parish; Larry E. Millikan, eds. (2012). Global Dermatology: Diagnosis and Management According to Geography, Climate, and Culture. M. Amer, R.A.C. Graham-Brown, S.N. Klaus, J.L. Pace. Springer Science & Business Media. p. 197\. ISBN 978-1461226147. Archived from the original on April 14, 2021. Retrieved May 17, 2014.
29. ↑ 29.0 29.1 “El indio en nuestro arte e histiografía”[permanent dead link], IFD de Minas, retrieved February 11, 2020.
30. ↑ 30.0 30.1 Magaña, Mario; Valerio, Julia; Mateo, Adriana; Magaña-Lozano, Mario (April 2005). "Alteraciones cutáneas del neonato en dos grupos de población de México" [Skin lesions two cohorts of newborns in Mexico City]. Boletín médico del Hospital Infantil de México (in español). 62 (2): 117–122. Archived from the original on 2021-06-30. Retrieved 2021-07-12.
31. ↑ “Tienen manchas mongólicas 50% de bebés” Archived 2020-06-01 at the Wayback Machine, El Universal, 16 de enero de 2012. Retrieved July 3, 2017.
32. ↑ Lewis B. Holmes (2011). Common Malformations. Oxford University Press. p. 414\. ISBN 9780195136029. Archived from the original on August 28, 2021. Retrieved October 27, 2019.
33. ↑ Castillo, F.; Bobbio, F. (June 1997). "Marcas cutáneas en recién nacidos" [Skin markings in newborns]. Dermatología Peruana (in español). 7 (1). Archived from the original on 2020-07-20. Retrieved 2021-07-12.
34. ↑ “Tienen manchas mongólicas 50% de bebés” Archived 2020-06-01 at the Wayback Machine, El Universal, January 2012. Retrieved on July 3, 2017.
35. ↑ Arturo Arias (2007). Taking Their Word: Literature and the Signs of Central America. U of Minnesota Press. p. 239\. ISBN 978-1452913162. Archived from the original on August 28, 2021. Retrieved May 17, 2014.
36. ↑ Herbert Goldhamer (2015). The Foreign Powers in Latin America. Princeton Legacy Library, Rand Corporation research study. Princeton University Press. p. 105\. ISBN 978-1400869152. Archived from the original on August 28, 2021. Retrieved May 17, 2014.
37. ↑ 尻 (in Japanese)
38. ↑ "The butt is blue": the untold story Archived 2013-10-05 at the Wayback Machine, Language Log Archived 2008-07-05 at the Wayback Machine, October 15, 2008.
39. ↑ Headley, Robert K. (1997). "Cambodian-English Dictionary". SEAlang Library. Archived from the original on January 27, 2009. Retrieved July 21, 2019.
40. ↑ "Life Magazine - Ancient and Modern Maya (June 1947)". Archived from the original on 2018-05-30. Retrieved 2021-07-12.
41. ↑ Eileen Maynard (1966). The Indians of Colta: Essays on the Colta Lake Zone, Chimborazo (Ecuador). Department of Anthropology, Cornell University. p. 6\. Archived from the original on August 28, 2021. Retrieved May 17, 2014.
42. ↑ Vox (2012). Vox Super-Mini Medical Spanish and English Dictionary. Vox dictionaries. McGraw Hill Professional. pp. 184, 121. ISBN 978-0071788632. Archived from the original on August 28, 2021. Retrieved May 17, 2014.

## External links[edit | edit source]

Classification|

* ICD-10: D22.5 (ILDS D22.505)
* ICD-9-CM: 757.33 (CDC/BPA 757.386)
* MeSH: D049328
* DiseasesDB: 8342

|

External resources|

* MedlinePlus: 001472
* eMedicine: derm/271

* v
* t
* e

Congenital malformations and deformations of integument / skin disease

Genodermatosis|

| Congenital ichthyosis/
erythrokeratodermia|

| AD|

* Ichthyosis vulgaris

|

AR|

* Congenital ichthyosiform erythroderma: Epidermolytic hyperkeratosis
* Lamellar ichthyosis
* Harlequin-type ichthyosis

* Netherton syndrome
* Zunich–Kaye syndrome
* Sjögren–Larsson syndrome

XR|

* X-linked ichthyosis

Ungrouped|

* Ichthyosis bullosa of Siemens
* Ichthyosis follicularis
* Ichthyosis prematurity syndrome
* Ichthyosis–sclerosing cholangitis syndrome
* Nonbullous congenital ichthyosiform erythroderma
* Ichthyosis linearis circumflexa
* Ichthyosis hystrix

and related|

* EBS
* EBS-K
* EBS-WC
* EBS-DM
* EBS-OG
* EBS-MD
* EBS-MP

* JEB
* JEB-H
* Mitis
* Generalized atrophic
* JEB-PA

* DEB
* DDEB
* RDEB

* related: Costello syndrome
* Kindler syndrome
* Laryngoonychocutaneous syndrome
* Skin fragility syndrome

Ectodermal dysplasia|

* Naegeli syndrome/Dermatopathia pigmentosa reticularis
* Hay–Wells syndrome
* Hypohidrotic ectodermal dysplasia
* Focal dermal hypoplasia
* Ellis–van Creveld syndrome
* Rapp–Hodgkin syndrome/Hay–Wells syndrome

Elastic/Connective|

* Ehlers–Danlos syndromes
* Cutis laxa (Gerodermia osteodysplastica)
* Popliteal pterygium syndrome
* Pseudoxanthoma elasticum
* Van der Woude syndrome

Hyperkeratosis/
keratinopathy|

| PPK|

* diffuse: Diffuse epidermolytic palmoplantar keratoderma
* Diffuse nonepidermolytic palmoplantar keratoderma
* Palmoplantar keratoderma of Sybert
* Meleda disease

* syndromic
* connexin
* Bart–Pumphrey syndrome
* Clouston's hidrotic ectodermal dysplasia
* Vohwinkel syndrome
* Corneodermatoosseous syndrome
* plakoglobin
* Naxos syndrome
* Scleroatrophic syndrome of Huriez
* Olmsted syndrome
* Cathepsin C
* Papillon–Lefèvre syndrome
* Haim–Munk syndrome
* Camisa disease
* focal: Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
* Focal palmoplantar and gingival keratosis
* Howel–Evans syndrome
* Pachyonychia congenita
* Pachyonychia congenita type I
* Pachyonychia congenita type II
* Striate palmoplantar keratoderma
* Tyrosinemia type II

* punctate: Acrokeratoelastoidosis of Costa
* Focal acral hyperkeratosis
* Keratosis punctata palmaris et plantaris
* Keratosis punctata of the palmar creases
* Schöpf–Schulz–Passarge syndrome
* Porokeratosis plantaris discreta
* Spiny keratoderma

* ungrouped: Palmoplantar keratoderma and spastic paraplegia
* desmoplakin
* Carvajal syndrome
* connexin
* Erythrokeratodermia variabilis
* HID/KID

|

Other|

* Meleda disease
* Keratosis pilaris
* ATP2A2
* Darier's disease
* Dyskeratosis congenita
* Lelis syndrome
* Dyskeratosis congenita
* Keratolytic winter erythema
* Keratosis follicularis spinulosa decalvans
* Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
* Keratosis pilaris atrophicans faciei

Other|

* cadherin
* EEM syndrome
* immune system
* Hereditary lymphedema
* Mastocytosis/Urticaria pigmentosa
* Hailey–Hailey

see also Template:Congenital malformations and deformations of skin appendages, Template:Phakomatoses, Template:Pigmentation disorders, Template:DNA replication and repair-deficiency disorder

Developmental
anomalies|

| Midline|

* Dermoid cyst
* Encephalocele
* Nasal glioma
* PHACE association
* Sinus pericranii

|

Nevus|

* Capillary hemangioma
* Port-wine stain
* Naevus simplex
* Nevus flammeus nuchae
* Midline nevus flammeus

Other/ungrouped|

* Aplasia cutis congenita
* Amniotic band syndrome
* Branchial cyst
* Cavernous venous malformation

* Accessory nail of the fifth toe
* Bronchogenic cyst
* Congenital cartilaginous rest of the neck
* Congenital hypertrophy of the lateral fold of the hallux
* Congenital lip pit
* Congenital malformations of the dermatoglyphs
* Congenital preauricular fistula
* Congenital smooth muscle hamartoma
* Cystic lymphatic malformation
* Median raphe cyst
* Melanotic neuroectodermal tumor of infancy
* Mongolian spot
* Nasolacrimal duct cyst
* Omphalomesenteric duct cyst
* Poland anomaly
* Rapidly involuting congenital hemangioma
* Rosenthal–Kloepfer syndrome
* Skin dimple
* Superficial lymphatic malformation
* Thyroglossal duct cyst
* Verrucous vascular malformation
* Birthmark

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